The role of [18F]PSMA-1007 PET/CT in staging of prostate cancer: Influence of bone uptake and relationship with D'Amico risk classification.

S S Medina-Ornelas, J E Vargas-Ahumada, R Hernandez-Ramirez, P Chavez-Torres, N Ramirez-Pedraza, A Leon-Alvarez, A Barrientos-Priego
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Abstract

Background: Prostate cancer represents a significant global health challenge, particularly in Mexico where it ranks as the leading cause of cancer-related mortality among men. The introduction of Prostate-Specific Membrane Antigen labeled with fluoride [18F]F-PSMA-1007 PET/CT has revolutionized diagnostics, enabling identification of metastases not visible on conventional imaging, although it presents unspecific bone uptake (UBU) in up to 72% of patients.

Methods: Eighty-one patients with newly diagnosed prostate cancer who underwent [18F]F-PSMA-1007 PET/CT for staging were retrospectively analyzed. Patients were categorized according to D'Amico risk classification. The prevalence of PSMA-positive lesions in various anatomical sites was assessed, defining unspecific bone uptake as focal uptake without meeting PROMISE criteria for osseous metastases.

Results: Metastatic disease, specifically defined by the presence of miN1 and/or miM1a-c lesions, was detected in a substantial majority of the patients, totaling 61 individuals, which corresponds to 75% of the entire cohort. Abnormal bone uptake was identified in 58% of cases, distributed equally across D'Amico risk groups. No significant association was found between bone uptake frequency and antigen prostatic specific (PSA) levels or Gleason score (p = 0.24). However, SUVmax was independently associated with metastasis (adjusted OR 1.67 per 5 units increase, 95% CI 1.31-2.14; p < 0.001). Definite bone metastases were confirmed in 44% of patients with bone uptake using an SUVmax ≥ 10 threshold.

Conclusions: [18F]F-PSMA-1007 PET/CT significantly enhances primary staging accuracy in prostate cancer, refining the D'Amico risk classification. The SUVmax ≥ 10 threshold allows differentiation between true bone metastases and unspecific bone uptake. Initial PSA levels significantly predict nodal metastases presence, optimizing treatment strategies and patient outcomes.

[18F]PSMA-1007 PET/CT在前列腺癌分期中的作用:骨摄取的影响及与D'Amico风险分级的关系
背景:前列腺癌是一项重大的全球健康挑战,特别是在墨西哥,它是男性癌症相关死亡的主要原因。引入前列腺特异性膜抗原标记氟化物[18F]F-PSMA-1007 PET/CT已经彻底改变了诊断方法,能够识别在常规影像学上不可见的转移,尽管它在高达72%的患者中呈现非特异性骨摄取(UBU)。方法:回顾性分析81例新诊断前列腺癌患者行[18F]F-PSMA-1007 PET/CT分期。根据D'Amico风险分级对患者进行分类。评估了psma阳性病变在不同解剖部位的患病率,将非特异性骨摄取定义为不符合骨转移PROMISE标准的局灶性摄取。结果:在绝大多数患者中检测到转移性疾病,具体定义为miN1和/或miM1a-c病变的存在,总共61例,相当于整个队列的75%。在58%的病例中发现了异常的骨摄取,在D'Amico风险组中分布均匀。骨摄取频率与前列腺抗原特异性(PSA)水平或Gleason评分无显著相关性(p = 0.24)。然而,SUVmax与转移独立相关(校正OR为1.67 / 5单位增加,95% CI为1.31-2.14;p)结论:[18F]F-PSMA-1007 PET/CT可显著提高前列腺癌的初级分期准确性,完善D'Amico风险分类。SUVmax≥10阈值可以区分真正的骨转移和非特异性骨摄取。初始PSA水平显著预测淋巴结转移的存在,优化治疗策略和患者预后。
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